BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Fetal, Acoustic

    PMA: P870025 · Supplement: S008 · Decision Mar 2, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Stimulator, Fetal, Acoustic
    Trade Name
    FETAL ACOUSTIC STIMULATOR
    PMA Number
    P870025
    Supplement Number
    S008
    Device Class
    FDA Class 3
    Product Code
    MCP
    Generic Name
    Stimulator, fetal, acoustic
    Medical Specialty
    Unknown
    Advisory Committee
    Obstetrics/Gynecology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    March 2, 2006
    Date Received
    August 1, 2005
    Supplement Type
    135 Review Track For 30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR VENDOR CHANGES FOR THE FOLLOWING COMPONENTS: DIE CAST FRAME AND PRINTED CIRCUIT BOARD (PCB) AND A CHANGE IN ADHESIVE MATERIAL.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MCP Stimulator, Fetal, Acoustic